ID
40255
Beschrijving
Study ID: 110635 Clinical Study ID: 110635 Study Title: A double-blind, randomized, placebo controlled, parallel group, multi-center, phase III trial of ofatumumab investigating clinical efficacy in adult patients with active rheumatoid arthritis who had an inadequate response to methotrexate therapy (FINAL ANALYSIS: follow-up period and cumulative safety data across the whole study) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00611455 Sponsor: GlaxoSmithKline Phase: Phase 3 Study Recruitment Status: Completed Generic Name: ofatumumab, Placebo Study Indication: Arthritis, Rheumatoid
Trefwoorden
Versies (1)
- 25-03-20 25-03-20 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
25 maart 2020
DOI
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Licentie
Creative Commons BY-NC 4.0
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Efficacy of ofatumumab in adult patients with active rheumatoid arthritis with inadequate response to methotrexate NCT00611455
Log Status; Non-Serious Adverse Events; Serious Adverse Events
- StudyEvent: ODM
Beschrijving
Non-Serious Adverse Event
Alias
- UMLS CUI-1
- C1518404
Beschrijving
Non-Serious Adverse Event - Sequence Number
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2348184
Beschrijving
Diagnosis Only (if known) Otherwise Sign/Symptom
Datatype
text
Alias
- UMLS CUI [1]
- C1518404
Beschrijving
Non-Serious Adverse Event - Modified term
Datatype
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2826798
Beschrijving
Non-Serious Adverse Event - MedDRA synonym
Datatype
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1140263
Beschrijving
Non-Serious Adverse Event - MedDRA lower level term code
Datatype
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C3898442
Beschrijving
Non-Serious Adverse Event - Failed coding
Datatype
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0805701
- UMLS CUI [1,3]
- C0231175
Beschrijving
Non-Serious Adverse Event - Start Date and Time
Datatype
datetime
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0808070
- UMLS CUI [1,3]
- C1301880
Beschrijving
Non-Serious Adverse Event - Outcome
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1705586
Beschrijving
Non-Serious Adverse Event - End Date and Time
Datatype
datetime
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0806020
- UMLS CUI [1,3]
- C1522314
Beschrijving
Non-Serious Adverse Event - Frequency
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0439603
Beschrijving
Non-Serious Adverse Event - Maximum Intensity
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0518690
- UMLS CUI [1,3]
- C0806909
Beschrijving
Non-Serious Adverse Event - Maximum Grade
Datatype
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0806909
Beschrijving
Non-Serious Adverse Event - Maximum Grade or Intensity
Datatype
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0806909
- UMLS CUI [1,4]
- C0518690
Beschrijving
Action Taken with Investigational Product(s) as a Result of the AE
Datatype
text
Alias
- UMLS CUI [1,1]
- C1704758
- UMLS CUI [1,2]
- C1518404
Beschrijving
Did the subject withdraw from study as a result of this AE?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1710677
- UMLS CUI [1,2]
- C1518404
Beschrijving
Use best judgment at initial entry. May be amended when additional information becomes available.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0013230
- UMLS CUI [1,3]
- C0439849
Beschrijving
Duration of AE if < 24 hours
Datatype
integer
Maateenheden
- h
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2926735
Beschrijving
Duration of AE if < 24 hours
Datatype
integer
Maateenheden
- min
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2926735
Beschrijving
Non-Serious Adverse Event - Time to Onset Since Last Dose
Datatype
integer
Maateenheden
- h
Alias
- UMLS CUI [1]
- C1518404
- UMLS CUI [2,1]
- C0332162
- UMLS CUI [2,2]
- C0040223
- UMLS CUI [2,3]
- C3174092
- UMLS CUI [2,4]
- C1517741
Beschrijving
Non-Serious Adverse Event - Time to Onset Since Last Dose
Datatype
integer
Maateenheden
- min
Alias
- UMLS CUI [1]
- C1518404
- UMLS CUI [2,1]
- C0332162
- UMLS CUI [2,2]
- C0040223
- UMLS CUI [2,3]
- C3174092
- UMLS CUI [2,4]
- C1517741
Beschrijving
Serious Adverse Event - Type of Report
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0585733
Beschrijving
Serious Adverse Event - Initial Report
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0684224
- UMLS CUI [1,3]
- C0205265
Beschrijving
Serious Adverse Event - Follow-Up Report
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1704685
- UMLS CUI [1,2]
- C1704685
Beschrijving
Serious Adverse Event - Randomisation
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0034656
Beschrijving
Serious Adverse Event
Alias
- UMLS CUI-1
- C1519255
Beschrijving
SAE Sequence Number
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2348184
Beschrijving
Diagnosis Only (if known) Otherwise Sign/Symptom Include ONE event term only
Datatype
text
Alias
- UMLS CUI [1]
- C1519255
Beschrijving
Serious Adverse Event - Modified Term
Datatype
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2826798
Beschrijving
Serious Adverse Event - MedDRA synonym
Datatype
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1140263
Beschrijving
Serious Adverse Event - MedDRA lower level term code
Datatype
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C3898442
Beschrijving
Serious Adverse Event - Failed Coding
Datatype
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0805701
- UMLS CUI [1,3]
- C0231175
Beschrijving
Serious Adverse Event - Start Date and Time
Datatype
datetime
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0808070
- UMLS CUI [1,3]
- C1301880
Beschrijving
Serious Adverse Event - Outcome
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1705586
Beschrijving
Serious Adverse Event - End Date and Time
Datatype
datetime
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0806020
- UMLS CUI [1,3]
- C1522314
Beschrijving
Serious Adverse Event - Date and Time of Death
Datatype
datetime
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1302234
- UMLS CUI [2]
- C1148348
- UMLS CUI [3]
- C1301931
Beschrijving
Serious Adverse Event - Maximum Intensity
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0518690
- UMLS CUI [1,3]
- C0806909
Beschrijving
Serious Adverse Event - Maximum Grade
Datatype
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0806909
Beschrijving
Serious Adverse Event - Maximum Grade or Intensity
Datatype
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0806909
- UMLS CUI [1,4]
- C0518690
Beschrijving
Action Taken with Investigational Product(s) as a Result of the SAE
Datatype
text
Alias
- UMLS CUI [1,1]
- C1704758
- UMLS CUI [1,2]
- C1519255
Beschrijving
Did the subject withdraw from study as a result of this SAE?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1710677
- UMLS CUI [1,2]
- C1519255
Beschrijving
Use best judgment at initial entry. May be amended when additional information becomes available.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0013230
- UMLS CUI [1,3]
- C0439849
Beschrijving
Serious Adverse Event - Duration of AE if < 24 hours
Datatype
integer
Maateenheden
- h
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0449238
Beschrijving
Serious Adverse Event - Duration of AE if < 24 hours
Datatype
text
Maateenheden
- min
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0449238
Beschrijving
Serious Adverse Event - Time to Onset Since Last Dose
Datatype
integer
Maateenheden
- h
Alias
- UMLS CUI [1]
- C1519255
- UMLS CUI [2,1]
- C0332162
- UMLS CUI [2,2]
- C0040223
- UMLS CUI [2,3]
- C3174092
- UMLS CUI [2,4]
- C1517741
Beschrijving
Serious Adverse Event - Time to Onset Since Last Dose
Datatype
integer
Maateenheden
- min
Alias
- UMLS CUI [1]
- C1519255
- UMLS CUI [2,1]
- C0332162
- UMLS CUI [2,2]
- C0040223
- UMLS CUI [2,3]
- C3174092
- UMLS CUI [2,4]
- C1517741
Beschrijving
Was the SAE caused by activities related to study participation other than investigational product?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2348568
- UMLS CUI [1,3]
- C0439849
- UMLS CUI [2,1]
- C0304229
- UMLS CUI [2,2]
- C0205394
- UMLS CUI [3]
- C2700391
- UMLS CUI [4]
- C0005834
- UMLS CUI [5]
- C1710661
Beschrijving
Was the event serious?
Datatype
boolean
Alias
- UMLS CUI [1]
- C1519255
Beschrijving
Serious Adverse Event - Related Investigational Product
Datatype
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0439849
- UMLS CUI [1,3]
- C0304229
Beschrijving
Serious Adverse Event - Seriousness
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C1710056
Beschrijving
Serious Adverse Event - Relevant Concomitant/ Treatment Medications
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C2347852
- UMLS CUI-3
- C0013227
Beschrijving
CM Sequence Number
Datatype
integer
Alias
- UMLS CUI [1,1]
- C2348184
- UMLS CUI [1,2]
- C2347852
Beschrijving
Enter drug name, not description (Generic name preferred. If combination product, enter Trade name).
Datatype
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C2360065
Beschrijving
Concomitant Medications - Modified reported term
Datatype
text
Alias
- UMLS CUI [1]
- C2826819
Beschrijving
Concomitant Medications - Dose
Datatype
integer
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C3174092
Beschrijving
Concomitant Medications - Unit
Datatype
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C1519795
Beschrijving
Concomitant Medications - Frequency
Datatype
text
Alias
- UMLS CUI [1,1]
- C3476109
- UMLS CUI [1,2]
- C2347852
Beschrijving
Concomitant Medications - Route
Datatype
text
Alias
- UMLS CUI [1]
- C2826730
Beschrijving
Concomitant Medications - Start Date
Datatype
date
Alias
- UMLS CUI [1]
- C2826734
Beschrijving
If no, specify End Date
Datatype
boolean
Alias
- UMLS CUI [1]
- C2826666
Beschrijving
Concomitant Medications - End date
Datatype
date
Alias
- UMLS CUI [1]
- C2826744
Beschrijving
Enter a medical diagnosis not description
Datatype
text
Alias
- UMLS CUI [1]
- C2826696
Beschrijving
Concomitant Medications - Modified reported term
Datatype
text
Alias
- UMLS CUI [1]
- C2826819
Beschrijving
Concomiant Medications - Drug Type
Datatype
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0457591
Beschrijving
Serious Adverse Event - Relevant Medical Conditions/Risk Factors
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0262926
- UMLS CUI-3
- C0035648
Beschrijving
MHx Sequence Number
Datatype
integer
Alias
- UMLS CUI [1,1]
- C2348184
- UMLS CUI [1,2]
- C0262926
Beschrijving
Enter a medical diagnosis not description.
Datatype
text
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C2348235
Beschrijving
Medical Condition - Modified reported term
Datatype
text
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C2826302
Beschrijving
If no, specify date of last occurrence
Datatype
text
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C0549178
Beschrijving
Medical Conditions - Date of last occurrence
Datatype
date
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C2745955
- UMLS CUI [1,3]
- C0011008
Beschrijving
Serious Adverse Event - Relevant Diagnostic Results
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C2347946
- UMLS CUI-3
- C0430022
- UMLS CUI-4
- C0456984
Beschrijving
Lab Sequence Number
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0022885
- UMLS CUI [1,2]
- C2348184
Beschrijving
Test Name
Datatype
text
Alias
- UMLS CUI [1]
- C0022885
Beschrijving
Test Date
Datatype
date
Alias
- UMLS CUI [1]
- C2826247
Beschrijving
Test Result
Datatype
text
Alias
- UMLS CUI [1]
- C0587081
Beschrijving
Test Units
Datatype
text
Alias
- UMLS CUI [1,1]
- C1519795
- UMLS CUI [1,2]
- C0587081
Beschrijving
Normal Low Range
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0086715
- UMLS CUI [1,2]
- C0205251
Beschrijving
Normal High Range
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0086715
- UMLS CUI [1,2]
- C0205250
Beschrijving
Relevant diagnostic results not noted above
Datatype
text
Alias
- UMLS CUI [1,1]
- C0587081
- UMLS CUI [1,2]
- C0205394
Beschrijving
Serious Adverse Event - Rechallenge
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C2347900
Beschrijving
If investigational product(s) were stopped temporarily, did the reported event(s) recur after investigational products were restarted?
Datatype
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0457454
- UMLS CUI [2,1]
- C0877248
- UMLS CUI [2,2]
- C0034897
- UMLS CUI [3]
- C0580673
Beschrijving
Serious Adverse Event - Investigational Product Double Blind Phase
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0304229
- UMLS CUI-3
- C0013072
Beschrijving
Double Blind Investigational product
Datatype
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0013072
Beschrijving
Double Blind Investigational product - Start Date
Datatype
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0013072
- UMLS CUI [1,3]
- C0808070
Beschrijving
Double Blind Investigational product - Stop Date
Datatype
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0013072
- UMLS CUI [1,3]
- C0806020
Beschrijving
Serious Adverse Event - Investigational Product Open Label Phase
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0304229
- UMLS CUI-3
- C3640652
Beschrijving
Study Drug
Datatype
text
Alias
- UMLS CUI [1]
- C0304229
Beschrijving
Start date of open label period
Datatype
date
Alias
- UMLS CUI [1,1]
- C3640652
- UMLS CUI [1,2]
- C0808070
Beschrijving
Open Label Course at time of event
Datatype
integer
Alias
- UMLS CUI [1,1]
- C3640652
- UMLS CUI [1,2]
- C0750729
- UMLS CUI [2]
- C0877248
Beschrijving
Open Label Phase - Start Date
Datatype
date
Alias
- UMLS CUI [1,1]
- C3640652
- UMLS CUI [1,2]
- C0808070
Beschrijving
Open Label Phase - Stop Date
Datatype
date
Alias
- UMLS CUI [1,1]
- C3640652
- UMLS CUI [1,2]
- C0806020
Beschrijving
Study Drug
Datatype
text
Alias
- UMLS CUI [1]
- C0304229
Beschrijving
Study Drug Start Date
Datatype
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0808070
Beschrijving
Study Drug Stop Date
Datatype
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0806020
Beschrijving
Study Drug Dose
Datatype
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0178602
Beschrijving
Study Drug Cumulative Dose
Datatype
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C2986497
Beschrijving
Serious Adverse Event - General Narrative Comments
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0947611
Beschrijving
Serious Adverse Event - Non Clinical
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0205210
- UMLS CUI-3
- C1298908
Beschrijving
Send incomplete SAE data to GSK Safety
Datatype
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1511726
- UMLS CUI [1,3]
- C0205257
Beschrijving
Receipt by GSK date
Datatype
datetime
Alias
- UMLS CUI [1]
- C2985846
Beschrijving
Was the event serious?
Datatype
boolean
Alias
- UMLS CUI [1]
- C1519255
Beschrijving
SAE Sequence Number
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2348184
Beschrijving
Version Number
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0333052
- UMLS CUI [1,2]
- C0237753
Beschrijving
Case ID
Datatype
text
Alias
- UMLS CUI [1,1]
- C1698493
- UMLS CUI [1,2]
- C0600091
Beschrijving
Randomisation Number
Datatype
text
Alias
- UMLS CUI [1,1]
- C0034656
- UMLS CUI [1,2]
- C0237753
Beschrijving
OCEANS Code
Datatype
text
Alias
- UMLS CUI [1]
- C0805701
Beschrijving
Email Flag
Datatype
text
Alias
- UMLS CUI [1]
- C0013849
Similar models
Log Status; Non-Serious Adverse Events; Serious Adverse Events
- StudyEvent: ODM
C0013227 (UMLS CUI [1,2])
C0347984 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C0347984 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C0347984 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C0347984 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C0347984 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C2348184 (UMLS CUI [1,2])
C2826798 (UMLS CUI [1,2])
C1140263 (UMLS CUI [1,2])
C3898442 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
C0808070 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,3])
C1705586 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C1522314 (UMLS CUI [1,3])
C0439603 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C0441800 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C0441800 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C0518690 (UMLS CUI [1,4])
C1518404 (UMLS CUI [1,2])
C1518404 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
C2926735 (UMLS CUI [1,2])
C2926735 (UMLS CUI [1,2])
C0332162 (UMLS CUI [2,1])
C0040223 (UMLS CUI [2,2])
C3174092 (UMLS CUI [2,3])
C1517741 (UMLS CUI [2,4])
C0332162 (UMLS CUI [2,1])
C0040223 (UMLS CUI [2,2])
C3174092 (UMLS CUI [2,3])
C1517741 (UMLS CUI [2,4])
C0585733 (UMLS CUI-2)
C0684224 (UMLS CUI [1,2])
C0205265 (UMLS CUI [1,3])
C1704685 (UMLS CUI [1,2])
C0034656 (UMLS CUI-2)
C0304229 (UMLS CUI [1,2])
C2348184 (UMLS CUI [1,2])
C2826798 (UMLS CUI [1,2])
C1140263 (UMLS CUI [1,2])
C3898442 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
C0808070 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,3])
C1705586 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C1522314 (UMLS CUI [1,3])
C1302234 (UMLS CUI [1,2])
C1148348 (UMLS CUI [2])
C1301931 (UMLS CUI [3])
C0518690 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C0441800 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C0441800 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C0518690 (UMLS CUI [1,4])
C1519255 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
C0449238 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
C0332162 (UMLS CUI [2,1])
C0040223 (UMLS CUI [2,2])
C3174092 (UMLS CUI [2,3])
C1517741 (UMLS CUI [2,4])
C0332162 (UMLS CUI [2,1])
C0040223 (UMLS CUI [2,2])
C3174092 (UMLS CUI [2,3])
C1517741 (UMLS CUI [2,4])
C2348568 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
C0304229 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
C2700391 (UMLS CUI [3])
C0005834 (UMLS CUI [4])
C1710661 (UMLS CUI [5])
C0439849 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,3])
C1710056 (UMLS CUI-2)
C0392360 (UMLS CUI [1,2])
C2347852 (UMLS CUI-2)
C0013227 (UMLS CUI-3)
C2347852 (UMLS CUI [1,2])
C2360065 (UMLS CUI [1,2])
C3174092 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,2])
C2347852 (UMLS CUI [1,2])
C0457591 (UMLS CUI [1,2])
C0262926 (UMLS CUI-2)
C0035648 (UMLS CUI-3)
C0262926 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,2])
C2826302 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,2])
C2745955 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C2347946 (UMLS CUI-2)
C0430022 (UMLS CUI-3)
C0456984 (UMLS CUI-4)
C2348184 (UMLS CUI [1,2])
C0587081 (UMLS CUI [1,2])
C0205251 (UMLS CUI [1,2])
C0205250 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C2347900 (UMLS CUI-2)
C0457454 (UMLS CUI [1,2])
C0877248 (UMLS CUI [2,1])
C0034897 (UMLS CUI [2,2])
C0580673 (UMLS CUI [3])
C0304229 (UMLS CUI-2)
C0013072 (UMLS CUI-3)
C0013072 (UMLS CUI [1,2])
C0013072 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
C0013072 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
C0304229 (UMLS CUI-2)
C3640652 (UMLS CUI-3)
C0808070 (UMLS CUI [1,2])
C0750729 (UMLS CUI [1,2])
C0877248 (UMLS CUI [2])
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,2])
C2986497 (UMLS CUI [1,2])
C0947611 (UMLS CUI-2)
C0205210 (UMLS CUI-2)
C1298908 (UMLS CUI-3)
C1511726 (UMLS CUI [1,2])
C0205257 (UMLS CUI [1,3])
C2348184 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,2])